Evidence map›Paper›PMID 30184340›Full record

ArticleStem cells translational medicine2019

Mesenchymal Stromal Cell-Seeded Biomimetic Scaffolds as a Factory of Soluble RANKL in Rankl-Deficient Osteopetrosis.

Ciro Menale, Elisabetta Campodoni, Eleonora Palagano, Stefano Mantero, Marco Erreni, Antonio Inforzato, Elena Fontana, Francesca Schena, Rob Van't Hof, Monica Sandri and 3 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Correction of osteopetrosis in the neonateFrontiers in endocrinology · 2024
    Article
  9. Review
  10. Review
  11. High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Review
  12. 3D Cocultures of Osteoblasts andPathogens (Basel, Switzerland) · 2021
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Ciro MenaleCNR-IRGB, Milan Unit, Milan, Italy.
Elisabetta CampodoniCNR-ISTEC, Faenza, Italy.
Eleonora PalaganoHumanitas Clinical and Research Institute, Rozzano, Italy.
Stefano ManteroCNR-IRGB, Milan Unit, Milan, Italy.
Marco ErreniHumanitas Clinical and Research Institute, Rozzano, Italy.
Antonio InforzatoHumanitas Clinical and Research Institute, Rozzano, Italy.
Elena FontanaCNR-IRGB, Milan Unit, Milan, Italy.
Francesca SchenaClinica Pediatrica e Reumatologia, UOSD Centro Malattie Autoinfiammatorie e Immunodeficienze, Genoa, Italy.
Rob Van't HofBone Research Group, Institute of Ageing & Chronic Disease, University of Liverpool, Liverpool, UK.
Monica SandriCNR-ISTEC, Faenza, Italy.
Anna TampieriCNR-ISTEC, Faenza, Italy.
Anna VillaCNR-IRGB, Milan Unit, Milan, Italy.
Cristina SobacchiCNR-IRGB, Milan Unit, Milan, Italy.ORCID 0000-0002-2684-7184
Humanitas University · ITInstitute of Genetic and Biomedical Research · ITInstitute of Science and Technology for Ceramics · ITAssociazione Italiana Sclerosi Multipla · ITUniversity of Liverpool · GBUniversity of Milan · IT

Funding

Medical Research Council MR/P020941/1
6 · The paper itself

Abstract

Biomimetic scaffolds are extremely versatile in terms of chemical composition and physical properties, which can be defined to accomplish specific applications. One property that can be added is the production/release of bioactive soluble factors, either directly from the biomaterial, or from cells embedded within the biomaterial. We reasoned that pursuing this strategy would be appropriate to setup a cell-based therapy for RANKL-deficient autosomal recessive osteopetrosis, a very rare skeletal genetic disease in which lack of the essential osteoclastogenic factor RANKL impedes osteoclast formation. The exogenously administered RANKL cytokine is effective in achieving osteoclast formation and function in vitro and in vivo, thus, we produced murine Rankl

Indexed as

BiomimeticsCell- and Tissue-Based TherapyHumansMesenchymal Stem CellsOsteopetrosisRANK LigandTissue EngineeringRANK LigandBiomimetic scaffoldCell therapyGene therapyMesenchymal stromal cellOsteopetrosisRANKL

Identifiers

PMID30184340
PMCPMC6312453
OpenAlexW2907594476

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.